ClinVar Miner

List of variants in gene combination ARMC5, LOC130058906 reported as likely benign for Cushing syndrome due to macronodular adrenal hyperplasia

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001105247.2(ARMC5):c.466C>T (p.Leu156Phe) rs114930262 0.00704

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